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Review of the PET/CT imaging patterns of treatment response in lymphoma [Meeting Abstract]

Karambelkar, A; Ghesani, M; Friedman, K
Objectives Learning objectives: 1. To review morphologic and functional imaging changes on PET/CT following various lymphoma treatment regimens. 2. To evaluate various circumstances under which the morphologic and functional imaging changes are concordant or discordant. The World Health Organization International Classification of Disease (2008) identifies numerous types of lymphoma based on histopathologic, immunohistochemical, cytogenetic, and molecular analyses. Practically, only a few subtypes of lymphoma account for the majority of cases such as diffuse large B cell lymphoma. Many of the lymphomas are potentially curable when treated with chemotherapy alone or in combination with radiation therapy; remainder are only potentially curable with stem cell transplantation. Nowadays PET/CT imaging is crucial in staging and treatment response assessment for most of these lymphomas. On PET/CT there are multiple imaging patterns of the treatment response. Additionally, there have been continuing efforts to establish the response criteria on PET/CT to help aid optimal treatment decisions. This exhibit is designed to review and understand the various imaging patterns observed on the PET/CT on treatment of the lymphoma following simple and complex treatment regimens
EMBASE:72335092
ISSN: 0161-5505
CID: 2187992

Phase II trial of exemestane with immunomodulatory oral cyclophosphamide in metastatic hormone receptor (HR)-positive breast cancer: Prolonged progression-free survival (PFS) in patients with distinct T regulatory cell (Treg) profile [Meeting Abstract]

Kwa, M; Novik, Y; Oratz, R; Jhaveri, K; Wu, J; Gu, P; Meyers, M; Muggia, F; Bonakdar, M; Abidoglu, C; Kozhaya, L; Li, X; Joseph, B; Iwano, A; Friedman, K; Goldberg, JD; Unutmaz, D; Adams, S
ISI:000375622400315
ISSN: 1538-7445
CID: 2411072

Outcome of small lung nodules missed on hybrid PET/MRI in patients with primary malignancy

Raad, Roy A; Friedman, Kent P; Heacock, Laura; Ponzo, Fabio; Melsaether, Amy; Chandarana, Hersh
PURPOSE: To assess outcomes of lung nodules missed on simultaneous positron emission tomography and magnetic resonance imaging (PET/MRI) compared to the reference standard PET and computed tomography (PET/CT) in patients with primary malignancy. MATERIALS AND METHODS: In all, 208 patients with primary malignancy undergoing clinically indicated (18 F) fluorodeoxyglucose (FDG) PET/CT followed by PET/MRI were independently reviewed by two readers. Upon review of the thoracic station on PET/MRI and PET/CT, 89 non-FDG avid small lung nodules in 43 patients were detected (by reader 1) only on the CT component of the PET/CT but were not identified on PET/MRI. Overall, 84 of these 89 nodules were examined on follow-up imaging with PET/CT or chest CT. The remaining five nodules had no follow-up imaging but had remote imaging available for comparison. RESULTS: Among the 84 nodules with follow-up, three nodules (3%) in one patient progressed, 10 (12%) nodules partially/completely resolved, whereas 71 nodules (85%) remained stable. The five nodules without follow-up were all stable since prior imaging of over 21 months. CONCLUSION: The vast majority (97%) of small non-FDG avid lung nodules missed on PET/MRI either resolved or remained stable on follow-up, suggestive of benignity. PET/MRI remains a viable alternative imaging modality in oncology patients, despite its low sensitivity in detecting small lung nodules. J. Magn. Reson. Imaging 2015.
PMID: 26192731
ISSN: 1522-2586
CID: 1683732

Current Status of Hybrid PET/MRI in Oncologic Imaging

Rosenkrantz, Andrew B; Friedman, Kent; Chandarana, Hersh; Melsaether, Amy; Moy, Linda; Ding, Yu-Shin; Jhaveri, Komal; Beltran, Luis; Jain, Rajan
OBJECTIVE: This review article explores recent advancements in PET/MRI for clinical oncologic imaging. CONCLUSION: Radiologists should understand the technical considerations that have made PET/MRI feasible within clinical workflows, the role of PET tracers for imaging various molecular targets in oncology, and advantages of hybrid PET/MRI compared with PET/CT. To facilitate this understanding, we discuss clinical examples (including gliomas, breast cancer, bone metastases, prostate cancer, bladder cancer, gynecologic malignancy, and lymphoma) as well as future directions, challenges, and areas for continued technical optimization for PET/MRI.
PMCID:4915069
PMID: 26491894
ISSN: 1546-3141
CID: 1810582

In Thyroidectomized Thyroid Cancer Patients, False-Positive I-131 Whole Body Scans Are Often Caused by Inflammation Rather Than Thyroid Cancer

Garger, Yana Basis; Winfeld, Mathew; Friedman, Kent; Blum, Manfred
Objective. To show that I-131 false-positive results on whole-body scans (WBSs) after thyroidectomy for thyroid cancer may be a result of inflammation unassociated with the cancer. Methods. We performed a retrospective image analysis of our database of thyroid cancer patients who underwent WBS from January 2008 to January 2012 to identify and stratify false positives. Results. A total of 564 patients underwent WBS during the study period; 96 patients were referred for 99 I-131 single-photon emission computed tomography (SPECT/CT) scans to better interpret cryptic findings. Among them, 73 scans were shown to be falsely positive; 40/73 or 54.7% of false-positive findings were a result of inflammation. Of the findings, 17 were in the head, 1 in the neck, 4 in the chest, 3 in the abdomen, and 14 in the pelvis; 1 had a knee abscess. Conclusions. In our series, inflammation caused the majority of false-positive WBSs. I-131 SPECT/CT is powerful in the differentiation of inflammation from thyroid cancer. By excluding metastatic disease, one can properly prognosticate outcome and avoid unnecessary, potentially harmful treatment of patients with thyroid cancer.
PMCID:4776247
PMID: 26977418
ISSN: 2324-7096
CID: 2031392

A phase I trial of ganetespib (heat shock protein 90 inhibitor) in combination with paclitaxel and trastuzumab in patients with human epidermal growth factor receptor-2 positive (HER2+) metastatic breast cancer (MBC) [Meeting Abstract]

Jhaveri, K; Teplinsky, E; Chandarlapaty, S; Solit, D; Cadoo, K; Speyer, J; D'Andrea, G; Adams, S; Patil, S; Haque, S; Friedman, K; Neville, D; Esteva, F; Hudis, C; Modi, S
ISI:000375622403294
ISSN: 1538-7445
CID: 2146992

Quantitative impact of Dixon mumap variability in dual-time-point brain PET/MR

Jackson, Kimberly; Bartlett, Rachel; Friedman, Kent; Shepherd, Timothy; Koesters, Thomas; Teruel, Jose; Fenchel, Mathias; Hermosillova-Valadez, Gerardo; Faul, David; Boada, Fernando
PMCID:4798694
PMID: 26956335
ISSN: 2197-7364
CID: 2023522

Tru-Cut Biopsy in Gynecologic Surgery

El Hachem, L; Mathews, S; Pereira, E; Momeni, M; Friedman, K; Chuang, L C; Gretz, H F 3rd
PMID: 27679040
ISSN: 1553-4669
CID: 2317052

Comparison of Coregistration Accuracy of Pelvic Structures Between Sequential and Simultaneous Imaging During Hybrid PET/MRI in Patients with Bladder Cancer

Rosenkrantz, Andrew B; Balar, Arjun V; Huang, William C; Jackson, Kimberly; Friedman, Kent P
PURPOSE: The aim of this study was to compare coregistration of the bladder wall, bladder masses, and pelvic lymph nodes between sequential and simultaneous PET and MRI acquisitions obtained during hybrid F-FDG PET/MRI performed using a diuresis protocol in bladder cancer patients. METHODS: Six bladder cancer patients underwent F-FDG hybrid PET/MRI, including IV Lasix administration and oral hydration, before imaging to achieve bladder clearance. Axial T2-weighted imaging (T2WI) was obtained approximately 40 minutes before PET ("sequential") and concurrently with PET ("simultaneous"). Three-dimensional spatial coordinates of the bladder wall, bladder masses, and pelvic lymph nodes were recorded for PET and T2WI. Distances between these locations on PET and T2WI sequences were computed and used to compare in-plane (x-y plane) and through-plane (z-axis) misregistration relative to PET between T2WI acquisitions. RESULTS: The bladder increased in volume between T2WI acquisitions (sequential, 176 [139]mL; simultaneous, 255 [146]mL). Four patients exhibited a bladder mass, all with increased activity (SUV, 9.5-38.4). Seven pelvic lymph nodes in 4 patients showed increased activity (SUV, 2.2-9.9). The bladder wall exhibited substantially less misregistration relative to PET for simultaneous, compared with sequential, acquisitions in in-plane (2.8 [3.1]mm vs 7.4 [9.1]mm) and through-plane (1.7 [2.2]mm vs 5.7 [9.6]mm) dimensions. Bladder masses exhibited slightly decreased misregistration for simultaneous, compared with sequential, acquisitions in in-plane (2.2 [1.4]mm vs 2.6 [1.9]mm) and through-plane (0.0 [0.0]mm vs 0.3 [0.8]mm) dimensions. FDG-avid lymph nodes exhibited slightly decreased in-plane misregistration (1.1 [0.8]mm vs 2.5 [0.6]mm), although identical through-plane misregistration (4.0 [1.9]mm vs 4.0 [2.8]mm). CONCLUSIONS: Using hybrid PET/MRI, simultaneous imaging substantially improved bladder wall coregistration and slightly improved coregistration of bladder masses and pelvic lymph nodes.
PMCID:4494885
PMID: 25783514
ISSN: 0363-9762
CID: 1506152

Practical guide for implementing hybrid PET/MR clinical service: lessons learned from our experience

Parikh, Nainesh; Friedman, Kent P; Shah, Shetal N; Chandarana, Hersh
Positron emission tomography (PET) and magnetic resonance imaging, until recently, have been performed on separate PET and MR systems with varying temporal delay between the two acquisitions. The interpretation of these two separately acquired studies requires cognitive fusion by radiologists/nuclear medicine physicians or dedicated and challenging post-processing. Recent advances in hardware and software with introduction of hybrid PET/MR systems have made it possible to acquire the PET and MR images simultaneously or near simultaneously. This review article serves as a road-map for clinical implementation of hybrid PET/MR systems and briefly discusses hardware systems, the personnel needs, safety and quality issues, and reimbursement topics based on experience at NYU Langone Medical Center and Cleveland Clinic.
PMCID:4534342
PMID: 25985966
ISSN: 1432-0509
CID: 1590672